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HRID 47504생성일: 2026년 10월 23일

Cyclohexanecarbonyl chloride → Cyclohexanecarboxamide

https://huagongshe.com/ko/reaction/47504

반응식

참여 물질

역할이름HCID투입량
반응물Cyclohexanecarbonyl chlorideHCID 75938—
반응물2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamineHCID 21946027—
생성물CyclohexanecarboxamideHCID 14283—

반응 단계

Using the general method of Example 92, cyclohexanecarbonyl chloride (94 μL, 0.7 mmol) was reacted with 2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethaneamine (0.2 g, 0.7 mmol) to provide 0.2 g of N12-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-1-cyclohexanecarboxamide as a white powder, m.p. 188-190° C. Analysis: Calculated for C22H30N6O: %C, 66.98; %H, 7.66; %N, 21.30. Found: %C, 66.72; %H, 7.57; %N, 21.48. HRMS (EI) calcd for C22H30N6O (M+) 394.2481 found 394.2475.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699878B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-152ace199404459786daa7d546210727
출처 메모uspto-grants-2004_03